Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Colorectal Surgery, Peking University Cancer Hospital & Institute, 52 Fucheng Road, Haidian District, Beijing, 100142, China.
Int J Colorectal Dis. 2012 Dec;27(12):1555-60. doi: 10.1007/s00384-012-1485-8. Epub 2012 May 30.
The purpose of this study was to analyze the prognostic value of vascular endothelial growth factor (VEGF) in patients with stage III rectal cancer treated with 30-Gy/10-fraction (f) preoperative radiotherapy and radical surgery.
One hundred and sixteen patients with clinical stage III rectal cancer were studied. All patients underwent radical surgery after 30-Gy/10-f preoperative radiotherapy. Immunohistochemical examination of VEGF was performed on the resected tumor specimen. An immunohistochemical score established from the extension and intensity of the markers was used for analysis. The log-rank test and proportional hazards regression analysis were used to calculate the probability that this biomarker was associated with patient outcomes.
The expression of VEGF was identified among 74.1 % (86 of 116) of patients. We found an increased incidence of distant metastasis (19.8 vs. 3.3 %, p = 0.039) and a decreased 3-year disease-free survival rate (96.7 % vs. 72.7 %, p = 0.003) in patients with positive VEGF staining. In multivariate survival analysis, positive VEGF staining (hazard ratio (HR) = 9.364, 95 % confidence interval (CI) 1.298-71.519, p = 0.027) and ypN+ stage (HR = 2.714, 95 % CI 1.419-3.331, p = 0.000) were the independent prognostic factors for disease-free survival. Subgroup analyses showed that the expression of VEGF was significantly associated with increased distant metastasis rate and decreased DFS in patients with ypN+ stage.
VEGF expression may have potential value for predicting distant metastasis and disease-free survival in stage III rectal cancer after 30-Gy/10-f preoperative radiotherapy. Inhibition of VEGF in combination with radiotherapy may improve the patient outcomes.
本研究旨在分析血管内皮生长因子(VEGF)在接受 30Gy/10 次(f)术前放疗和根治性手术治疗的 III 期直肠癌患者中的预后价值。
对 116 例临床 III 期直肠癌患者进行研究。所有患者均在接受 30Gy/10 次术前放疗后接受根治性手术。对切除的肿瘤标本进行 VEGF 的免疫组织化学检查。使用从标志物的扩展和强度建立的免疫组织化学评分进行分析。使用对数秩检验和比例风险回归分析计算该生物标志物与患者结局相关的概率。
在 116 例患者中,有 74.1%(86 例)的患者存在 VEGF 表达。我们发现,VEGF 阳性染色患者的远处转移发生率增加(19.8%比 3.3%,p=0.039),3 年无病生存率降低(96.7%比 72.7%,p=0.003)。多变量生存分析显示,VEGF 阳性染色(风险比(HR)=9.364,95%置信区间(CI)1.298-71.519,p=0.027)和ypN+期(HR=2.714,95%CI 1.419-3.331,p=0.000)是无病生存的独立预后因素。亚组分析显示,VEGF 表达与 ypN+期患者远处转移率增加和无病生存时间降低显著相关。
VEGF 表达可能对预测接受 30Gy/10 次术前放疗的 III 期直肠癌患者的远处转移和无病生存具有潜在价值。VEGF 抑制与放疗联合可能改善患者的结局。